UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.53822126_53822127delinsGT , CM000672.2:g.53822126_53822127delinsGT | GRCh38 |
| NC_000010.10:g.55581886_55581887delinsGT , CM000672.1:g.55581886_55581887delinsGT | GRCh37 |
| NC_000010.9:g.55251892_55251893delinsGT | NCBI36 |
| NG_009191.2:g.984165_984166delinsAC | |
| NG_009191.3:g.1812056_1812057delinsAC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000613657.6:c.4409+3009_4409+3010delinsAC | ENSP00000482794.1:n.4409+3009_4409+3010de... | |
| ENST00000320301.11:c.5599_5600delinsAC MANE Plus Clinical | ENSP00000322604.6:p.Thr1867= | |
| ENST00000395445.6:c.4388+5266_4388+5267delinsAC | ENSP00000378832.2:n.4388+5266_4388+5267de... | |
| ENST00000613657.5:c.4409+3009_4409+3010delinsAC | ENSP00000482794.1:n.4409+3009_4409+3010de... | |
| ENST00000642496.1:c.3227-1897_3227-1896delinsAC | ||
| ENST00000644397.2:c.4368-1897_4368-1896delinsAC MANE Select | ENSP00000495195.1:n.4368-1897_4368-1896de... | |
| ENST00000320301.10:c.5599_5600delinsAC | ENSP00000322604.6:p.Thr1867= | |
| ENST00000361849.7:c.5605_5606delinsAC | ENSP00000354950.3:p.Thr1869= | |
| ENST00000373956.7:c.*3554_*3555delinsAC | ENSP00000363067.4:n.*3554_*3555delinsAC | |
| ENST00000373957.7:c.5620_5621delinsAC | ENSP00000363068.4:p.Thr1874= | |
| ENST00000373965.6:c.4373+3009_4373+3010delinsAC | ENSP00000363076.3:n.4373+3009_4373+3010de... | |
| ENST00000395430.5:c.5590_5591delinsAC | ENSP00000378818.1:p.Thr1864= | |
| ENST00000395432.6:c.5479_5480delinsAC | ENSP00000378820.2:p.Thr1827= | |
| ENST00000395433.5:c.5530_5531delinsAC | ENSP00000378821.1:p.Thr1844= | |
| ENST00000395438.5:c.4371+5265_4371+5266delinsAC | ENSP00000378826.2:n.4371+5265_4371+5266de... | |
| ENST00000395440.5:c.1306-12581_1306-12580delinsAC | ENSP00000378827.1:n.1306-12581_1306-12580... | |
| ENST00000395442.5:c.1099-12581_1099-12580delinsAC | ENSP00000378829.1:n.1099-12581_1099-12580... | |
| ENST00000395445.5:c.4388+5266_4388+5267delinsAC | ENSP00000378832.2:n.4388+5266_4388+5267de... | |
| ENST00000395446.5:c.2092-12581_2092-12580delinsAC | ENSP00000378833.1:n.2092-12581_2092-12580... | |
| ENST00000409834.5:c.3206+3009_3206+3010delinsAC | ENSP00000386693.1:n.3206+3009_3206+3010de... | |
| ENST00000414367.5:c.*447+5266_*447+5267delinsAC | ENSP00000412531.1:n.*447+5266_*447+5267de... | |
| ENST00000414778.5:c.4370+5266_4370+5267delinsAC | ENSP00000410304.2:n.4370+5266_4370+5267de... | |
| ENST00000437009.5:c.5392_5393delinsAC | ENSP00000412628.2:p.Thr1798= | |
| ENST00000448885.5:c.*3560_*3561delinsAC | ENSP00000412320.1:n.*3560_*3561delinsAC | |
| ENST00000463095.2:n.2618_2619delinsAC | ||
| ENST00000495484.5:c.462-4114_462-4113delinsAC | ENSP00000480780.1:n.462-4114_462-4113deli... | |
| ENST00000612394.4:c.4406+5266_4406+5267delinsAC | ENSP00000482921.1:n.4406+5266_4406+5267de... | |
| ENST00000613657.4:c.4409+3009_4409+3010delinsAC | ENSP00000482794.1:n.4409+3009_4409+3010de... | |
| ENST00000614895.4:c.4385+5266_4385+5267delinsAC | ENSP00000478512.1:n.4385+5266_4385+5267de... | |
| ENST00000616114.4:c.4367+5266_4367+5267delinsAC | ENSP00000483745.1:n.4367+5266_4367+5267de... | |
| ENST00000617051.4:c.5626_5627delinsAC | ENSP00000484703.1:p.Thr1876= | |
| ENST00000617271.4:c.4373+3009_4373+3010delinsAC | ENSP00000478076.1:n.4373+3009_4373+3010de... | |
| ENST00000618301.4:c.594-4114_594-4113delinsAC | ENSP00000482780.1:n.594-4114_594-4113deli... | |
| ENST00000621708.4:c.4388+3009_4388+3010delinsAC | ENSP00000484454.1:n.4388+3009_4388+3010de... | |
| ENST00000622048.4:c.5398_5399delinsAC | ENSP00000482329.1:p.Thr1800= | |
| NM_001142763.1:c.5620_5621delinsAC | NP_001136235.1:p.Thr1874= | |
| NM_001142764.1:c.5605_5606delinsAC | NP_001136236.1:p.Thr1869= | |
| NM_001142765.1:c.5392_5393delinsAC | NP_001136237.1:p.Thr1798= | |
| NM_001142766.1:c.5590_5591delinsAC | NP_001136238.1:p.Thr1864= | |
| NM_001142767.1:c.5479_5480delinsAC | NP_001136239.1:p.Thr1827= | |
| NM_001142768.1:c.5539_5540delinsAC | NP_001136240.1:p.Thr1847= | |
| NM_001142769.1:c.4409+3009_4409+3010delinsAC | NP_001136241.1:n.4409+3009_4409+3010delin... | |
| NM_001142770.1:c.4373+3009_4373+3010delinsAC | NP_001136242.1:n.4373+3009_4373+3010delin... | |
| NM_001142771.1:c.4388+3009_4388+3010delinsAC | NP_001136243.1:n.4388+3009_4388+3010delin... | |
| NM_001142772.1:c.4373+3009_4373+3010delinsAC | NP_001136244.1:n.4373+3009_4373+3010delin... | |
| NM_001142773.1:c.5530_5531delinsAC | NP_001136245.1:p.Thr1844= | |
| NM_033056.3:c.5599_5600delinsAC | NP_149045.3:p.Thr1867= | |
| NM_001142769.2:c.4409+3009_4409+3010delinsAC | NP_001136241.1:n.4409+3009_4409+3010delin... | |
| NM_001142770.2:c.4373+3009_4373+3010delinsAC | NP_001136242.1:n.4373+3009_4373+3010delin... | |
| NM_001354404.1:c.5533_5534delinsAC | NP_001341333.1:p.Thr1845= | |
| NM_001354411.1:c.4388+5266_4388+5267delinsAC | NP_001341340.1:n.4388+5266_4388+5267delin... | |
| NM_001354420.1:c.4367+5266_4367+5267delinsAC | NP_001341349.1:n.4367+5266_4367+5267delin... | |
| NM_001354429.1:c.4368-4114_4368-4113delinsAC | NP_001341358.1:n.4368-4114_4368-4113delin... | |
| XM_017016573.2:c.4388+3009_4388+3010delinsAC | XP_016872062.1:n.4388+3009_4388+3010delin... | |
| XR_001747192.2:n.6612_6613delinsAC | ||
| XR_001747193.2:n.6603_6604delinsAC | ||
| NM_001142763.2:c.5620_5621delinsAC | NP_001136235.1:p.Thr1874= | |
| NM_001142764.2:c.5605_5606delinsAC | NP_001136236.1:p.Thr1869= | |
| NM_001142765.2:c.5392_5393delinsAC | NP_001136237.1:p.Thr1798= | |
| NM_001142766.2:c.5590_5591delinsAC | NP_001136238.1:p.Thr1864= | |
| NM_001142768.2:c.5539_5540delinsAC | NP_001136240.1:p.Thr1847= | |
| NM_001142769.3:c.4409+3009_4409+3010delinsAC | NP_001136241.1:n.4409+3009_4409+3010delin... | |
| NM_001142770.3:c.4373+3009_4373+3010delinsAC | NP_001136242.1:n.4373+3009_4373+3010delin... | |
| NM_001142771.2:c.4388+3009_4388+3010delinsAC | NP_001136243.1:n.4388+3009_4388+3010delin... | |
| NM_001142772.2:c.4373+3009_4373+3010delinsAC | NP_001136244.1:n.4373+3009_4373+3010delin... | |
| NM_001142773.2:c.5530_5531delinsAC | NP_001136245.1:p.Thr1844= | |
| NM_001354411.2:c.4388+5266_4388+5267delinsAC | NP_001341340.1:n.4388+5266_4388+5267delin... | |
| NM_001354420.2:c.4367+5266_4367+5267delinsAC | NP_001341349.1:n.4367+5266_4367+5267delin... | |
| NM_001354429.2:c.4368-4114_4368-4113delinsAC | NP_001341358.1:n.4368-4114_4368-4113delin... | |
| NM_033056.4:c.5599_5600delinsAC MANE Plus Clinical | NP_149045.3:p.Thr1867= | |
| NM_001142767.2:c.5479_5480delinsAC | NP_001136239.1:p.Thr1827= | |
| NM_001354404.2:c.5533_5534delinsAC | NP_001341333.1:p.Thr1845= | |
| NM_001384140.1:c.4368-1897_4368-1896delinsAC MANE Select | NP_001371069.1:n.4368-1897_4368-1896delin... |